Abstract
Although surgical excision, chemo-, and radio-therapy are clearly advanced, tumors may relapse due to cells of the so-called “minimal residual disease”. Indeed, small clusters of tumor cells persist in host tissues after treatment of the primary tumor elaborating strategies to survive and escape from immunological attacks before their relapse: this variable period of remission is known as “cancer dormancy”. Therefore, it is crucial to understand and consider the major concepts addressing dormancy, to identify new targets and disclose potential clinical strategies. Here, we have particularly focused the relationships between tumor microenvironment and cancer dormancy, looking at a re-appreciated aspect of this compartment that is the low extracellular pH. Accumulating evidences indicate that acidity of tumor microenvironment is associated with a poor prognosis of tumor-bearing patients, stimulates a chemo- and radio-therapy resistant phenotype, and suppresses the tumoricidal activity of cytotoxic lymphocytes and natural killer cells, and all these aspects are useful for dormancy. Therefore, this review discusses the possibility that acidity of tumor microenvironment may provide a new, not previously suggested, adequate milieu for “dormancy” of tumor cells.
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Introduction
Early detection and new therapeutic approaches drastically improve cure and progression-free survival of tumor-bearing patients. In general, a detectable primary tumor is treated by chemotherapy, surgery, and/or radiation leading to its elimination from the patient or reduction in size to a few viable cells. However, survival of a small number of malignant cells, the so-called “minimal residual disease”, might arise for diverse reasons, including an incomplete surgical excision for impossible diagnosis of too small clusters of cells. Furthermore, tumor cells might survive to chemotherapeutic and radiotherapeutic treatments, depending on the variability of cell cycle length and phase of each single cell, or depending on the expression of a drug resistant phenotype. Surviving cells may have different fates, consisting of starting again to grow or entering into a “dormant state”. Thus, it is possible for tumor cells to persist for extended periods until the host dies. Otherwise, after a prolonged period of time corresponding to clinical remission, tumor cell can give rise to a secondary lesion. Those lesions may occur locally or at distant site from the pre-existing primary tumor and are known as organ metastasis. The emergence of metastasis is, indeed, the most dangerous event during the natural history of the neoplastic disease. Although only a minority of patients exhibit clinically detectable metastases at the time of diagnosis, metastases are responsible for more than 90% of patient mortality. Metastatic lesions result from a multistep process that involves progression of tumor cells into primary host tissues, intravasation into altered tumoral blood vessels, and dissemination to distant organs, and extravasation and growth after adaptation into the foreign tissue microenvironment. The term “dormancy” indicates the length of time needed to metastatic cells for adaption to secondary organs [1]. Clinical observations report that melanoma, breast, and prostate tumors may relapse into target organs many years or decades after apparent curative treatment of primary tumor. This is possible because tumor cells spread to distant organs earlier than we may expect and survive in the hostile new microenvironments. Isolation of disseminated tumor cells in the blood by liquid biopsy may help to prevent and combat this behaviour. Other clinical reports describe extraordinarily long remissions following surgical treatment of intraocular melanoma, testicular teratoma, osteogenic sarcoma, and renal carcinoma [2]. During the dormant state, tumor cells survive in the host tissues remaining confined in a low proliferating or quiescent state, resisting to drugs and immune attacks, until being recruited into a high proliferation compartment by either genetic or epigenetic changes. Dormancy may be sustained by limited blood supply; this condition of low oxygen and reduced nutrients determines an absolute increase of tumor cells number very close to zero, since the number of dividing cells may equate the number of dying cells [3, 4]. It is important to remember that many of the mechanisms proposed to explain dormancy have been identified using experimental models, although all are very plausible, up to now are not completely confirmed in tumor-bearing patients [1]. Thus, it is important to introduce new hypotheses and offer new tools to improve knowledge regarding tumor dormancy, to translate these new advances into clinic.
This review discusses the relevance of a particular aspect of tumor microenvironment, participating in harbouring dormant tumor cells, either from primary or secondary lesions. The aspect of tumor microenvironment which we are interested to introduce in the complex scenario of dormancy is represented by the extracellular acidosis, which frequently characterizes solid tumors.
Why tumor microenvironment is often characterized by low pH
Tumor cells, even when there is enough O2 to support mitochondrial function, use glycolysis to sustain their high proliferation rate, the so-called “Warburg effect” [5, 6]. This phenomenon was first reported by O.H. Warburg in the 1920s, and although the “Warburg hypothesis” of impaired mitochondrial metabolism has proven to be incorrect, an increased conversion of glucose to lactic acid and H+ in tumors has been constantly demonstrated. “Aerobic glycolysis” leads to the conversion of one molecule of glucose into two molecules of lactic acid and 2 H+ to produce 2 ATP, compared to the 36 ATP produced by oxidative metabolism [5, 6]. Thus, ATP generation from glycolysis is far less efficient, although rapidity of this pathway might represent a compensatory aspect. Furthermore, tumor cells implement glycolysis promoting an abnormal high rate of glucose uptake [7] trough the up-regulation and the enhanced activity of glucose transporters. The increased glucose uptake is useful for diagnostic purposes, as in the case of monitoring uptake of glucose analogue tracer (18F)-fluoro-2-deoxy-d-glucose (18FdG) by positron-emission tomography (PET) [8]. PET imaging of tumor-bearing patients has shown that numerous, although not all, primary and metastatic lesions express a significant glucose uptake.
Aerobic glycolysis up-regulation in malignant phenotype, that is mostly due to stable genetic or epigenetic changes [5], is important for proliferating tumor cells since glucose can be diverted into macromolecular precursors. Indeed, glucose 6-phosphate is used for glycogen and ribose 5-phosphate biosynthesis, dihydroxyacetone phosphate for triacylglycerol and phospholipid synthesis, and pyruvate for alanine and malate synthesis. Furthermore, the isoform of pyruvate kinase M2, usually highly expressed in tumor cells under activity of oncogenic transcription factor c-MYC, may slow down aerobic glycolysis, which results into accumulation of up-stream precursors for anabolic demand of proliferating cells [9]. c-MYC is also involved in promotion of many of glycolytic enzymes [10], together with Akt pathway, which enhances glycolysis through activation of hexokinase 2, phosphofructokinase 1 and 2 and expression of glucose transporters [11–13]. The generated pyruvate, together with the entry of glutamine into tricarboxylic acid (TCA) cycle, cooperates to the promotion of anabolic reactions needed for cell division. Thus, an enhanced lactic acid production during a high rate of proliferation is difficult to imagine, and only when uptake of glucose superimposes anabolic biomass formation, lactic acid starts to accumulate and extracellular pH reduces. A high glycolytic rate has an additional advantage for proliferating tumor cells, that is the reduction of radical oxidative substances and the related cytotoxic effects [14].
When oxygen tension decreases and a hypoxic microenvironment develops, stabilization of hypoxia inducible factor 1α (HIF-1α) transcription factor may regulate an elevated number of genes driving tumor cells metabolism toward an anaerobic glycolysis pathway. Such genes include glucose transporters (GLUT1 and 3) [15], glycolytic enzymes (Hexokinase I and II, phosphofructokinase-1, aldolase-A and C, phosphoglycerate kinase 1, enolase-α), pyruvate dehydrogenase kinase 1 (PDK1, that inactivates the enzyme responsible for conversion of pyruvate to acetyl-CoA [16]), and genes for lactate production (LDHA, encoding lactate dehydrogenase A, which converts pyruvate to lactate [17]) and for lactate extrusion (MTC-4, the monocarboxylate transporter-4). Lactate production in hypoxic cancer cells is also enhanced by the increased expression of PKM2 [18] and activation of PDK1. PDK1 suppresses pyruvate dehydrogenase (PDH) activity limiting the entry of pyruvate into TCA cycle. Thus, pyruvate is mostly redirected into lactate and H+ by LDH-A.
Therefore, to maintain an intracellular pH compatible with survival and/or proliferation, additional adaptations are required. The mechanism for long-term internal pH control is represented by promotion in tumor cells of multiple and redundant families of transporters, which release protons and lactate into extracellular environment, such as: Na+/H+ exchanger 1 (NHE1), HCO3 − transporters (Na+/HCO3 − co-transporters, NBCs and anion exchange protein 1, AE1), proton-linked monocarboxylate transporters (MCT1 and 4), and vacuolar H+-ATPases (V-ATPases) [19]. In addition, carbonic anhydrases IX (CAIX), a hypoxia–inducible effector, participates to the complex machinery responsible of internal pH control favouring export of protons and import of bicarbonate ions [19].
On the whole, cancer cells that adapt their metabolism to different levels of oxygen caused by either dividing process or hypoxic condition produce a significant acidification of the extracellular microenvironment. It is known that pH value of extracellular environment in several tumor histotype ranges from 6.7 to 7.1 [20]. Interestingly, extracellular acidosis maintains a high level of CAIX expression in tumor cells, in a HIF-1α-independent way [21]. Furthermore, we cannot exclude that tumor extracellular acidity may also be supported by a poor blood perfusion and an uneven distribution of lymphatic vessels, frequently very poor in the core of the mass and more evident in the periphery. As a consequence, interstitial fluid pressure is maintained elevated. It is for these considerations that acidosis of the extracellular space of tumors has been included among the most important hallmarks of tumor microenvironment [22].
How low pH may contribute to dormancy of tumor cells
Acidity induces a reduced proliferation, high resistance to apoptosis and autophagy
Whereas a coordinate series of events account for progression through the cell cycle in normal cells, in cancer cells, the deregulation of multiple control mechanisms results in different degrees of autonomy from growth-stimulatory or -inhibitory signals, making cancer cells adapted to grow quite indefinitely. However, proliferative rate of tumor cells may vary and non/slow-proliferating cells are common, which implies a high rate of cell death. Indeed, studies of human and animal tumors have demonstrated heterogeneity in mitotic index within different regions of the same tumor mass. The heterogeneity of cell proliferation is due to different factors, such as cell differentiation, variant generation with different proliferative rates, and availability of oxygen and nutrients (i.e., glucose, glutamine, and branched-chain amino acids) in the microenvironment. Thus, slow-proliferating cells may occur in solid tumors and often are responsible for relapse, due to their high resistance to clinical treatments. In this context, acidic tumor microenvironment promotes in tumor cells a low-proliferating phenotype, which does not revert even in the presence of a high level of growth factors [23]. It has also been shown by several reports that extracellular acidosis increases the percentage of cells in G0 phase [24]. Indeed, exposure to acidosis alters growth factor signaling and reduces serum ability to stimulate Raf/ERK/mTORC1 kinase pathway [25]. Aguirre-Ghiso et al. showed that dormancy in human head and neck cancer cells depends on the block of the Raf/ERK pathway together with the activation of p38 [26]. Besides, it was demonstrated that acidity inhibits AMPK [27] driving a mitotic delay through a misoriented spindle due to improper astral microtubule-cell cortex interactions [28]; indeed, it is known that cell division is achieved through a correct assembly, positioning, and orientation of the microtubule-based spindle. Extracellular acidity modulates intracellular pH that in turn directly affects cell cycle. This is a quite common mechanism for cell proliferation control in both normal and cancer cells that was demonstrated several years ago [29]. When internal pH drops following a sustained extracellular acidosis, also G2/M entry is limited by a reduced cyclin-dependent kinase 1-cyclin B1 activity [30].
A recent study showed that transforming growth factor-β2 (TGFβ2) was effective in promoting the up-regulation of p27 and p38 by the SMAD1/2/5 pathway in tumor cells undergoing a dormant state [31]. Lactic acid was shown to induce both transcription and protein secretion of TGFβ2 in glioma cells [32] and to induce TGFβ1 production in in vivo model [33]. More recently, we found that an acidic microenvironment is able to promote TGFβ secretion and signaling in mesenchymal stem cells (MSC), driving the progression to malignancy in a melanoma cell system [34] and suggesting that acidity is a strong inducer of TGFβ family members. Esomeprazole, a proton pump inhibitor activated by acidity, inhibited TGFβ expression in MSC grown in a low pH medium [34].
In addition, we have observed that a reduced pH promotes in melanoma cells a typical epithelial-to-mesenchymal transition (EMT) program characterized by a reduced level of proliferation, induction of several mesenchymal markers, resistance to apoptosis and high metalloprotease-dependent invasiveness [35]. Acidosis-exposed tumor cells were also able to favour in vivo organ colonization of intravenously injected non-acidic tumor cells, indicative of a new cooperation between tumor cell subpopulations [35]. We may suggest that acidic-adapted melanoma cells protect non-acidic cells from blood turbulence and possible interactions with immune cells, and support survival and final lodgment in host microenvironment of secondary organ. Furthermore, acidity contributes to promote in melanoma cells an elevated resistance to pro-apoptotic agents [35] and resistance to apoptosis is well ascertained to be useful for dormant tumor cells. Additional evidences indicate that low pH activates MAPK signaling in a variety of tumor cells generating a protective effect against apoptosis induced by multiple cytotoxic stresses [36, 37]. Incubation of lymphoma cells in acidic conditions (pH 6.5) blocks apoptosis promoted by glucose or glutamine deprivation, a phenomenon mediated by the acid-sensing G protein-coupled receptor (GPR65) through an up-regulation of Bcl-2 and Bcl-xL factors [38]. Thus, it is possible that the reduction of tumor mass expansion during dormancy favoured by acidity will be a consequence of a delay of the cell cycle, rather than the induction of cell death.
Another aspect associated with EMT elicited in tumor cells by acidity is represented by their metabolic adaptation. Acidic cancer cells switch from glycolysis to oxidative phosphorylation (Oxphos) to favour a generation of more bioenergetic molecules instead of biomass for cell division [27, 39]. Metformin, a standard drug for diabetes, is a very efficient drug to kill acidic melanoma cells inhibiting their metabolic program [27]. The main energetic source of acidic pH-adapted cancer cells was identified to derive from fatty acid oxidation [40]. An acidic niche is able to preserve Oxphos metabolism in tumor cells also in high glucose, indicating the absence of Crabtree effect in acidic cells [41]. Oxphos metabolism might be convenient for dormant cells which need energy to survive and resist several stressors using alternative substrates. Furthermore, it has been observed that quiescent human leukaemia stem cells use Oxphos to produce the required energy [42].
Despite the liaison between acidic phenotype and stemness is still not completely clear, an indication of a possible connection can consist in the fact that EMT induces stem-like traits in different tumor types, such as mammary tumors [43] and head and neck squamous cell carcinoma [44]. Acidity, independently from a restricted oxygen tension, promotes stem cell markers and self-renewal in glioma cells. Low pH exerts a promotion of glioma stem cells (GSC) through elaboration of HIF-2α-dependent angiogenic factors. Induction of HIF-2α and other GSC markers by acidic stress can be reverted by pH elevation, suggesting that GSC phenotype might be targeted, raising pHe [45]. Lisanti et al. [46] found that ketones and lactate stimulate stem cell markers in breast carcinoma cells, expressing an oxidative mitochondrial metabolism. This suggests that an appropriate mitochondrial antagonist, such as metformin, could eradicate cancer stem cell subpopulation. Hirsch et al. [47] showed that metformin selectively kills cancer stem cells isolated from breast cancer, and the combination between metformin and doxorubicin kills both cancer stem cells and non-stem cancer cells and prevents relapse much more efficiently than either drug alone in a xenograft mouse model. Quite recently, Petrachi et al. demonstrated that phenphormin, but not metformin, is able to affect viability and growth of melanoma cancer stem cells [48].
An additional tumor survival mechanism, also important for dormancy, is autophagy. Autophagy is a catabolic process through which cellular metabolism is maintained recycling the self-digested cytoplasmic proteins and organelles. Low levels of autophagic activity are observed under physiological conditions, while in tumor cells, autophagy promotes cell survival during the frequent nutrient restriction and hypoxia [49]. Autophagy was found to sustain the maintenance of cancer stem cell phenotype, and cooperates to chemo- and radio-resistance [50–53]. Inhibition of autophagy, on the contrary, increases chemo- and radio-sensitivity [54]. Acute and chronic exposure to low pH promotes high level of autophagic activity, and this sustains cell survival and aggressiveness, while the pharmacological inhibition of autophagy in such acidic tumor cells reduces their ability to survive [55]. Furthermore, it was demonstrated that acidosis blocks the inhibitory activity of chloroquine on autophagy, thus chloroquine does not result effective in tumor treatment [56]. Up-regulation of autophagy-mediated degradation and recycling of cellular substrates by acidic cancer cells can support metabolic pathways considering that an acidic microenvironment is generally characterized by low nutrients and oxygen.
Finally, it seems reasonable to suggest that the phenotype acquired by acidic tumor cells results into several characteristics useful for a dormant state, such as low replication rate, high resistance to apoptosis and autophagy.
Acidity promotes invasion
Acid-activated tumoral catepsin L was reported to be able to amplify proteinase cascade through activation of urokinase-type plasminogen activator (uPA) [57], which converts plasminogen to plasmin. This latter then degrades various components of the extracellular matrix (ECM), such as fibronectin, laminin, proteoglycan, and collagen [58], and activates latent collagenase and growth factors [59]. The concomitant expression of uPA and uPA receptor (uPAR) by tumor cells results in a high invasive capability [60]. uPAR is a glycosylphosphatidyl-inositol (GPI)-anchored molecule, and therefore, it lacks transmembrane domains able to transfer extracellular signals to signaling pathways. Thus, uPAR must cooperate with cell membrane molecules able to confer signaling competence on uPAR itself [61]. Upon interaction of α chain with uPAR, integrins α5β1 and αvβ3 can interact and activate Receptor Tyrosine Kinases (RTKs). Such interaction is potentiated by catalytic and non-catalytic uPA binding to uPAR and can induce RTKs activity even in the absence of the relevant ligand (EGF, PDGF, ILGF, and HGF) [61, 62] in an FAK-dependent manner [63]. In head and neck carcinoma, uPAR drives tumor growth by interacting with α5β1 integrin, a complex that activates focal adhesion kinase (FAK) and EGF receptor (EGFR), final effector of this mitogenic signal. Blocking uPAR, β1-integrin, FAK or EGFR, singly or in combination, results in tumor growth suppression and dormancy [1]. Indeed, it was reported that dormancy associates with a quite complete inhibition of the Raf-MEK-ERK pathway as in quiescent cells [64]. Therefore, it is reasonable that, even though uPAR is up-regulated in acidity, its mitogenic activity may be abrogated by loss of integrin interaction and/or reduction in EGFR cross talk. This last condition may leave uPAR to exert pro-invasive effects without promoting cell proliferation.
Furthermore, acid-activated cathepsin B and cathepsin-activated uPA/plasminogen/plasmin axis activate secreted latent metallo-proteases (MMPs) by proteolytic cleavage. MMPs are a family of structurally related zinc-dependent endopeptidases, collectively capable of degrading all components of ECM [65]. MMPs have long been associated with invasiveness, angiogenesis and tumor cell dissemination [66–68], due to their capacity to help tumor cells to cross-structural barriers, including basement membranes, to migrate into the blood, extravasate and colonize in distant host tissues. Kato et al. have shown that, in mouse metastatic B16 melanoma cells, expression of MMP-9 and in vitro invasiveness is induced by acidic pHe (pHe 5.4–6.5) [69]. Another component of basement membrane to be degraded by tumor cells to disseminate is the heparan sulphate chains. Toyoshima and Nakajima reported that heparanase has an optimal pH of 4.2, but a significant heparanase activity persists at pH 6.0–6.5, suggesting that the acidic environment of tumors may activate the degrading properties of tumor heparanases [70].
When melanoma cells were exposed to acidic condition for long time and selected subpopulations were isolated, it was found that these tumor cells exhibit a high level of invasiveness and proliferation following re-exposure to physiological pH [71]. The high level of invasiveness and proliferation of acid-adapted tumor cells after exposure to the standard pH evokes the awaking of dormant tumor cells, invasion in local host tissues, and growth.
In contrast to the several findings on the positive relationship between acidity and invasiveness, it is still under debate whether low pH may promote motility, the so-called amoeboid style of migration. Stock et al. using a model of directional cell migration in an extracellular pH gradient showed that melanoma cells hardly migrate at pHe 6.6 when adhesion was found particularly elevated [72]. Indeed, through computational molecular dynamic simulations, Paradise et al. found that acidic extracellular pH (pH 6.0 for 8 h) promotes opening of the αvβ3 headpiece [73], a conformational change supporting a stable interaction between integrin αvβ3 and its ECM biological ligands. In accordance, we experienced that acidity-exposed melanoma cells reduce their ability to heal wounds, tested by scratch test analysis, and express a reduced capacity to cross filters of Boyden chambers. Only when we exposed melanoma cells to lactic acid, migration recovers the level of control melanoma cells grown in the standard pH medium, however, without exceeding it [27].
Acidity may participate to dormancy either conferring, during the initial period of adaptation of tumor cells into the foreign microenvironment, some invasive properties useful to lodge in new sites, or favouring growth into adjacent host tissues when some genetic or epigenetic changes induce relapse.
Acidity promotes angiogenesis
Regarding angiogenesis, it was demonstrated that a transient exposure of endometrial carcinoma cells to acidosis (8 h at pH 5.5) induced a preferential VEFG121 isoform up-regulation through p38 MAPK and SAPK/JNK pathways [74]. When human pancreatic adenocarcinoma cells were incubated for different periods at pH between 6.7 and 7.4, it was found that the expression of VEGF was particularly stimulated by a 6–8 h-pH 6.7–7.1 treatment. Acidic pH also simulates NF-kB binding activity to the NF-kB site of VEGF [75, 76]. NF-kB was also found responsible of acidic pH-induced transcriptional activation of IL-8 gene, a promoter of angiogenesis [77]. However, when breast carcinoma cells were exposed to a pH 6.7 for 18 h, there was a significant decrease in VEGF mRNA expression [78]. Acidosis may also play an inhibitory role on angiogenesis exerting a potent block on HIF-1α stabilization, a key hypoxia transcription factor involved in VEGF gene activation [79]. Thus, angiogenesis regulation by pH might be either tissue specific or time of exposure-dependent, considering that acute acidosis stimulates, whereas a chronic exposure inhibits VEGF.
By studying acidosis-induced signalings in tumor cells, we observed that extracellular acidity (pH 6.7 ± 0.1) stimulates the expression and secretion of lymphangiogenic growth factor C (VEGF-C) by melanoma cells, mediated by NF-κB transcription factor activity [80]. We also demonstrated that esomeprazole, a proton pump inhibitor (PPI) activated by a low pH, inhibits VEGF-C expression in acidic melanoma cells down-regulating NF-κB [80]. VEGF-C, in addition to the well-known role of VEGF-A in relapse, might represent a new causal link between lymphangiogenesis, lymph node colonization, and progression [81]. Development of new lymphatic vessels might be also instrumental in reducing the high interstitial pressure expressed by certain tumor regions, favouring diffusion of macromolecules from blood vessels to tumor cells, which may relapse.
During a dormant period, quiescent or low-proliferating cells may take advantage to express a pro-angiogenic and/or lymphangiogenic phenotype that an acidic microenvironment may stimulate to finely control level of nutrients.
Acidity favours escaping from immune surveillance
To explain time variability of dormant state, Aguirre-Ghiso JA has proposed three major mechanisms: cellular dormancy, angiogenic dormancy, and immunosurveillance [1]. During cellular dormancy, tumor cells are G0–G1 arrested and they need to evade immune cell cytotoxicity to survive. Genetic modifications can re-activate a proliferative activity, even at low rate, in dormant cells. Despite this, the expansion of tumor lesion may not be reached, due to the effect of an active immune response and to the balance between pro- and anti-angiogenic. We believe that tumor microenvironment acidosis may sustain cellular dormancy, maintaining tumor cells unable to resume proliferation and hiding them from immune surveillance.
There is increasing evidence that cancer cells escape immune destruction by suppressing the anti-cancer immune response through maintaining a relatively low pH in their environment [82]. Indeed, the acquired acidic phenotype enables cancer cells to suppress the anti-cancer activity of immune cells promoting the secretion of chemokines to enhance T-regulatory recruitment or producing immunosuppressive cytokines [83]. Several studies have shown that acidic pHe inhibits T-cell proliferation [84], dendritic cell maturation [85], cytotoxic T lymphocyte activity (CTLs) [86], lymphokine-activated killer cells [87], and natural killer (NK) activity and viability [88]. Furthermore, lowering pHe to 6.5 has been reported to lead to a loss of function of human and murine tumor-infiltrating T lymphocytes consisting in a significant impairment of cytolytic activity, cytokine secretion, and reduction of T-cell receptor and interleukin-2 α-chain receptor expression [89]. T-cell function was found to be completely restored buffering pH to a physiological value; however when exposure to an acidic microenvironment was sufficiently prolonged, such as a chronic exposure, T cells were deeply damaged and underwent apoptosis [89].
Extracellular lactic acid generated by glycolytic cancer metabolism and accumulated in tumor microenvironment supports the suppressive effect on T-cell function exerted by low pH [83]. Mendler et al. identified that tumor lactic acidosis suppresses CTL functions via inhibition of p38 and JNK/c-Jun activation [90] and Fisher et al. demonstrated that lactic acid inhibits T-cell proliferation in a dose-dependent manner, whereas sodium lactate, which does not lead to an acidification of the medium, had no suppressive effect [84]. Moreover, prolonged incubation with high dose of lactic acid (20 mM) was shown to induce CTL death of up to 60%, while exposure to the same low pH, derived from HCl addition to the medium, was less effective. It has also been demonstrated that lactic acid generated by cancer cells promotes tumor development by inhibiting the immune response increasing arginase-1 (ARG1) expression and inducing IL-23/IL-17 secretion by tumor-associated macrophages (TAMs) of M2 phenotype [91]. Indeed, transient exposure of cells to acidic pH suppresses the ability of macrophages to mount an adequate antibacterial response elicited by Toll-like receptor 2 and 4 activation [92].
Recent studies indicate that buffering low pH at the tumor site by in vivo administration of esomeprazole, a PPI, improves tumor-infiltrating lymphocyte effector functions in melanoma lesions and delays cancer progression in tumor-bearing mice [89, 93]. Inhibition of proton pumps on tumor cells with pantoprazole, another PPI, hampers tumor-induced suppression of macrophages both in vitro and in vivo [94, 95]. Finally, neutralization of tumor pH with bicarbonate impairs the growth of cancer in mice, and this effect was associated with an increased T-cell infiltration in tumor masses [96].
Overall, several evidences sustain that low pH might provide an immunological privileged niche functional for cellular dormancy of quiescent tumor cells.
Acidity promotes resistance to drug and radio-treatment
Acidosis is able to influence the resistance of tumor cells to anticancer therapy [97], one of the major obstacle during chemotherapeutic treatment of solid tumors [98]. Cellular drug uptake and intracellular targeting are key factors for a successful anticancer treatment and both mechanisms are influenced by pHe. Extracellular acidity reduces the intracellular concentration of chemotherapeutic agents, mainly weak base drugs, through a mechanism termed “ion trapping”, and based on ion protonation of drugs [99–102]. Thus, the reversion of this pH gradient may strongly facilitate the successful treatment. Indeed, several in vitro and in vivo studies show that low pH reduces uptake and efficacy of weak base chemotherapeutics, such as anthracyclines (e.g., doxorubicin), anthraquinones (e.g., mitoxantrone), and vinca alkaloids (e.g., vincristine and vinblastine) [101, 103]. On the contrary, alkalization of extracellular environment enhances intracellular accumulation and cytotoxicity of some of these weak base drugs [104]. Accordingly, Wojtkowiak et al. demonstrated that a combined treatment with sodium bicarbonate and doxorubicin reduces more efficiently tumor volume than doxorubicin alone [105], suggesting that alkalization enhances doxorubicin efficacy. According to these results, De Milito and Fais showed that in vivo oral pretreatment with proton pump inhibitors (PPIs) of tumor-bearing animals re-sensitizes tumors to anticancer drugs [106].
Other possible mechanisms working on drug resistance in low pH have been described. Among these, it is of a great importance the ability of acidic pHe to increase the pump activity of the p-glycoprotein (pGP), a drug efflux transporter. Thews et al. observed that acidic prostate carcinoma cells express a pGP activity more than doubled of that of cells grown in a standard pH medium [107]. These authors reported that up-regulation of pGP in acidic cells was related to an increased intracellular Ca2+ level, stimulated by a protein kinase C activity [107]. It has also been observed that acidosis-induced pGP activity may be related to ERK and p38 pathways. The inhibition of both ERK and p38 abolished acidosis-induced daunorubicin efflux and re-establish daunorubicin sensitivity in rat prostate cancer cells [108]. Moreover, acidosis of the extracellular milieu may interfere in drug efficacy inducing a cell quiescence, namely, inducing a very low proliferative rate, as previously discussed [35, 97, 109]. It is known that cells are more sensitive to drugs and radiation therapy when in S-phase than in the other cell cycle phases. Tumor pH may also have indirect effects on cell sensitivity to drugs; actually, chronic exposure to an acidic pH is reported to increase expression of heat shock protein HSP27 level in tumor cells, leading to resistance to cisplatin [110].
Studying the effects of irradiation on cell killing and induction of apoptosis on low pH (pH 6.8) adapted human maxillary carcinoma cells, Ohtsubo et al. found that these cells, chronically adapted to low pHe, express a radio-insensitive phenotype [111]. To support this finding, it was found that an acidic microenvironment induces p53 expression [112], suppresses radiation-induced apoptosis [113, 114], and prolongs radiation-induced G2/M arrest, resulting in an increased DNA damage repair during the prolonged G2 arrest [115].
On the whole, acidity of extracellular microenvironment confers to dormant tumor cells a great advantage sustaining a resistant chemo- and radio-therapy phenotype, and treatments aimed to buffer extracellular acidity may revert several aggressive properties including resistance to conventional therapy.
Concluding remarks
Acidosis of tumor microenvironment of most solid tumors is well ascertained to promote an aggressive, immune-, chemo-, and radio-resistant phenotype, and in some circumstances an EMT program and stemness (Fig. 1). Therefore, acidic-adapted tumor cells are likely be able to survive to endogenous and exogenous stressors and might represent a hidden reserve of tumor cells from which a tumor could relapse and disseminate. Thus, acidosis of solid tumors may acquire a role in generating a novel niche of dormant tumor cells. Along with this view, it is reasonable for a successful treatment of cancer to build up new combined strategies focused on the inhibition of tumor cell-microenvironment crosstalk, and in particular targeting acidosis and acidic-adapted tumor cells.
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This study was financially supported by grants from Istituto Toscano Tumori, Ente Cassa di Risparmio di Firenze.
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Peppicelli, S., Andreucci, E., Ruzzolini, J. et al. The acidic microenvironment as a possible niche of dormant tumor cells. Cell. Mol. Life Sci. 74, 2761–2771 (2017). https://doi.org/10.1007/s00018-017-2496-y
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DOI: https://doi.org/10.1007/s00018-017-2496-y